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Status |
Public on Oct 13, 2021 |
Title |
H2A.Z RELACS of ZGA staged embryos |
Organism |
Drosophila melanogaster |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
During embryogenesis, the genome shifts from transcriptionally quiescent to extensively active in a process known as Zygotic Genome Activation (ZGA). In Drosophila, the pioneer factor Zelda is known to be essential for the progression of development, still, it regulates the activation of only a small subset of genes at ZGA. However, thousands of genes do not require Zelda, suggesting that other mechanisms exist. By conducting GRO-seq, HiC and ChIP-seq in Drosophila embryos, we demonstrate that up to 65% of zygotically activated genes are enriched for the histone variant H2A.Z and independent of Zelda. H2A.Z enrichment precedes ZGA and Polymerase II loading onto chromatin. In vivo knock-down of maternally contributed Domino, a histone chaperone and ATPase, reduces H2A.Z deposition at transcription start sites, causes global downregulation of housekeeping genes at ZGA, and compromises the establishment of the 3D chromatin structure. We infer that maternal factors and H2A.Z are master regulators of the de novo establishment of transcriptional programs during ZGA via chromatin reorganization.
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Overall design |
Corresponding Inputs and H2A.Z RELACS ChIP-seq in Ctrl and DomKD ZGA embryos, 2 replicates per condition
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Contributor(s) |
Ibarra Morales DA, Iovino N |
Citation(s) |
34853314 |
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Submission date |
Nov 16, 2020 |
Last update date |
Jan 12, 2022 |
Contact name |
Nicola Iovino |
E-mail(s) |
[email protected]
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Organization name |
MPI of Immunobiology and Epigenetics
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Street address |
Stübeweg 51
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City |
Freiburg |
ZIP/Postal code |
79108 |
Country |
Germany |
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Platforms (1) |
GPL23323 |
Illumina HiSeq 3000 (Drosophila melanogaster) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE161594 |
Histone variant H2A.Z regulates zygotic genome activation |
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Relations |
BioProject |
PRJNA678810 |
SRA |
SRP292840 |